A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564383



Internal ID16351792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37754070..37793557hg38UCSC Ensembl
Innerchr14:38223275..38262762hg19UCSC Ensembl
Innerchr14:37293026..37332513hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3839488
hg1939488
hg1839488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3643n54
Supporting Variantsnssv825977
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564383
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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